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HRID 48978作成日:2026年10月24日

Pyridine → 3-(3,5-Dimethylpyrazol-1-yl)-5-nitro-1,2-benzisothiazole

https://huagongshe.com/ja/reaction/48978

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物3,5-DimethylpyrazoleHCID 6210—
反応物1,2-Benzisothiazole, 3-chloro-5-nitro-HCID 198098—
溶媒Ethyl AcetateHCID 8857—
生成物3-(3,5-Dimethylpyrazol-1-yl)-5-nitro-1,2-benzisothiazoleHCID 2063426643.8%

反応手順

A mixture of 3-chloro-5-nitrobenzisothiazole (5.3 g, mmol), 3,5-dimethylpyrazole (2.40 g, 25.0 mmol) and pyridine is stirred overnight at reflux, cooled to room temperature and diluted with ethyl acetate. The resultant mixture is filtered and the filtrate is washed with three portions of 10% hydrochloric acid and one portion of water. The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuo to afford the title compound (2.85 g, 43.8%) which is identified by NMR spectral analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706663B2
出典データセットuspto-grants-2004_03
ORD IDord-2faec26a94d54e92a133e6d5e439322b
出典メモuspto-grants-2004_03